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机构地区:[1]中国药科大学中药复方研究室,南京211198
出 处:《中国实验方剂学杂志》2011年第6期74-76,共3页Chinese Journal of Experimental Traditional Medical Formulae
摘 要:目的:建立HPLC同时测定乳癖消颗粒中芍药苷、三七皂苷R1、人参皂苷Rg1、连翘苷、哈巴俄苷、人参皂苷Rb1、去氢木香内酯7种成分的含量。方法:采用AlltimaC18色谱柱(4.6 mm×250 mm,5μm);乙腈-水为流动相,梯度洗脱,检测波长203 nm,柱温30℃,流速1.0 mL·min-1。结果:芍药苷、三七皂苷R1、人参皂苷Rg1、连翘苷、哈巴俄苷、人参皂苷Rb1、去氢木香内酯线性范围分别为3.906 25~125μg(r=0.999),9.375~300μg(r=0.999),37.5~1 200μg(r=1.000),2.187 5~70μg(r=0.999),3.75~120μg(r=0.999),25~800μg(r=0.999),0.625~20μg(r=1.000);平均加样回收率分别为97.95%(RSD 0.71%),99.05%(RSD 1.11%),100.70%(RSD 2.46%),102.74%(RSD 0.35%),103.06%(RSD 0.55%),98.25%(RSD 1.68%),100.16%(RSD 1.82%)。结论:本方法方便、稳定、可靠,可用于乳癖消颗粒的质量控制。Objective:To establish a method for simultaneous determination of seven components such as paeoniflorin,ginsenoside R1,ginsenoside Rg1,forsythin,harpagoside,ginsenoside Rb,dehydrocostuslactone contained in Rupixiao granule.Method:HPLC was conducted on an Alltima C18 column(4.6 mm × 250 mm,5 μm) at 30 ℃;the mobile phase was consisted of acetonitrile(A)-water(B) with gradient elution at the flow rate of 1.0 mL·min^-1 detected at 203 nm.Result:The linear range(mg·L^-1) of paeoniflorin,ginsenoside R1,ginsenoside Rg1,forsythin,harpagoside,ginsenoside Rb,dehydrocostuslactone was 3.906 25-125(r = 0.999),9.375-300(r = 0.999),37.5-1 200(r = 1.000),2.1875-70(r = 0.999),3.75-120(r = 0.999),25-800(r = 0.999) and 0.625-20 μg(r = 1.000) respectively.The average recoveries were 97.95%(RSD 0.71%),99.05%(RSD 1.11%),100.70%(RSD 2.46%),102.74%(RSD 0.35%),103.06%(RSD 0.55%),98.25%(RSD 1.68%) and 100.16%(RSD 1.82%) respectively.Conclusion:The developed method was convenient,reliable and accurate for the quality control of Rupixiao preparation.
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